Canonical Allele Identifier: CA400557871

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566050C>A (hg19) ; chr17:g.63488689C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488689C>A , CM000679.2:g.63488689C>A	GRCh38
NC_000017.10:g.61566050C>A , CM000679.1:g.61566050C>A	GRCh37
NC_000017.9:g.58919782C>A	NCBI36
NG_011648.1:g.16617C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2347C>A MANE Select	ENSP00000290866.4:p.Leu783Met
ENST00000290863.10:c.625C>A	ENSP00000290863.6:p.Leu209Met
ENST00000290866.9:c.2347C>A	ENSP00000290866.4:p.Leu783Met
ENST00000413513.7:c.625C>A	ENSP00000392247.3:p.Leu209Met
ENST00000428043.5:c.2347C>A	ENSP00000397593.2:p.Leu783Met
ENST00000577647.2:c.625C>A	ENSP00000464149.1:p.Leu209Met
ENST00000578839.5:c.*417C>A	ENSP00000462110.2:n.*417C>A
ENST00000579204.1:c.606C>A	ENSP00000464629.1:n.606C>A
ENST00000579314.5:c.*76C>A	ENSP00000462599.1:n.*76C>A
ENST00000582005.5:c.*267C>A	ENSP00000462002.1:n.*267C>A
ENST00000582761.1:c.115C>A	ENSP00000462909.1:p.Leu39Met
ENST00000584865.5:n.293C>A
NM_000789.3:c.2347C>A	NP_000780.1:p.Leu783Met
NM_001178057.1:c.625C>A	NP_001171528.1:p.Leu209Met
NM_152830.2:c.625C>A	NP_690043.1:p.Leu209Met
XM_005257110.1:c.1798C>A	XP_005257167.1:p.Leu600Met
XM_006721737.2:c.685C>A	XP_006721800.2:p.Leu229Met
XM_006721737.3:c.685C>A	XP_006721800.2:p.Leu229Met
NM_000789.4:c.2347C>A MANE Select	NP_000780.1:p.Leu783Met
NM_001178057.2:c.625C>A	NP_001171528.1:p.Leu209Met
NM_152830.3:c.625C>A	NP_690043.1:p.Leu209Met
NM_001382700.1:c.1780C>A	NP_001369629.1:p.Leu594Met
NM_001382701.1:c.1495C>A	NP_001369630.1:p.Leu499Met
NM_001382702.1:c.277C>A	NP_001369631.1:p.Leu93Met
NR_168483.1:n.725C>A